Proyecto para la creación de una microempresa productora y comercializadora de productos cuyo principal ingrediente es la machica

If certification of devices under the MDR has not been finalised before expiry of the Directive’s certificate, and where the device does not present an unacceptable risk to health

The notified body that issued the AIMDD or MDD certificate may confirm in writing (after having reviewed manufacturer’s description of the (proposed) change) that the

 Tejidos de origen humano o sus derivados que sean inviables o hayan sido transformados en inviables con una función accesoria..  Células de origen humano o sus derivados que

d) que haya «identidad de órgano» (con identidad de Sala y Sección); e) que haya alteridad, es decir, que las sentencias aportadas sean de persona distinta a la recurrente, e) que

Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in

Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in

This section provides guidance with examples on encoding medicinal product packaging information, together with the relationship between Pack Size, Package Item (container)

Package Item (Container) Type : Vial (100000073563) Quantity Operator: equal to (100000000049) Package Item (Container) Quantity : 1 Material : Glass type I (200000003204)